Evidence map›Paper›PMID 18992405›Full record

ReviewThe Lancet. Infectious diseases2008

Vaginal microbicides and the prevention of HIV transmission.

Blayne Cutler, Jessica Justman

Open access · greenAbstract readReview
In one paragraph

Review in The Lancet. Infectious diseases, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 73 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
73citing papers in PubMed, 3 pooled it
16.4field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

73 citing papers in PubMed, 3 syntheses or guidelines pooled it, 170 citations in OpenAlex.

  1. Topical microbicides for preventing sexually transmitted infections.The Cochrane database of systematic reviews · 2021
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  20. Poly(ethylene glycol) (PEG)-lactic acid nanocarrier-based degradable hydrogels for restoring the vaginal microenvironment.Journal of controlled release : official journal of the Controlled Release Society · 2014
    Article

13 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors at 1 institution in 1 country.

Blayne CutlerDepartment of Medicine, Mailman School of Public Health, Columbia University, New York, NY 10032, USA.
Jessica Justman
Columbia University · US

Funding

Centers for Innovative Research to Control AIDSU01AI069466 · NIAID · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI EL-SADR, WAFAA M. · 2007 to 2011
$14.0M
HIV PREVENTION TRIAL UNIT (PRIDE NYC PROGRAM)U01AI048016 · NIAID · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI EL-SADR, WAFAA M. · 2000 to 2006
$7.8M
Training in the Epidemiology of Infectious DiseasesT32AI049821 · NIAID · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI EL-SADR, WAFAA M. · 2001 to 2010
$2.5M
NIAID NIH HHS 5T32 AI049821NIAID NIH HHS 5U01 AI048016NIAID NIH HHS AI 48016NIAID NIH HHS T32 AI049821NIAID NIH HHS U01 AI048016NIAID NIH HHS U01 AI069466
6 · The paper itself

Abstract

Worldwide, nearly half of all individuals living with HIV are now women, who acquire the virus largely by heterosexual exposure. With an HIV vaccine likely to be years away, topical microbicide formulations applied vaginally or rectally are being investigated as another strategy for HIV prevention. A review of preclinical and clinical research on the development of microbicides formulated to prevent vaginal HIV transmission yielded 118 studies: 73 preclinical and 45 clinical. Preclinical research included in-vitro assays and cervical explant models, as well as animal models. Clinical research included phase I and II/IIb safety studies, and phase III efficacy studies. Whereas most phase I and phase II clinical trials have found microbicide compounds to be safe and well tolerated, phase III trials completed to date have not demonstrated efficacy in preventing HIV transmission. Topical microbicides are grouped into five classes of agents, based on where they disrupt the pathway of sexual transmission of HIV. These classes include surfactants/membrane disruptors, vaginal milieu protectors, viral entry inhibitors, reverse transcriptase inhibitors, and a fifth group whose mechanism is unknown. The trajectory of microbicide development has been toward agents that block more specific virus-host cell interactions. Microbicide clinical trials face scientifically and ethically complex issues, such as the choice of placebo gel, the potential for viral resistance, and the inclusion of HIV-infected participants. Assessment of combination agents will most likely advance this field of research.

Indexed as

Administration, IntravaginalAnti-Retroviral AgentsClinical Trials as TopicFemaleHIVHIV InfectionsHumansMaleSurface-Active AgentsVaginaVaginal Creams, Foams, and JelliesAnti-Retroviral AgentsSurface-Active AgentsVaginal Creams, Foams, and Jellies

Identifiers

PMID18992405
PMCPMC2627483
OpenAlexW2167246391

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.